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1 nce of molecular motors - a process we term 'skating'.
2 the homologue in a primitive vertebrate, the skate.
3 elios, and Eos in Raja eglanteria (clearnose skate), a cartilaginous fish that is representative of a
4                                        Three skate AE isoforms (skAEs) are expressed, and at least sk
5 e ability of the basic domain of dynactin to skate along microtubules is used by dynein to maintain l
6            Prominent expression of Ikaros in skate also is found in the lymphoid Leydig organ and epi
7 rall most closely resembles mu chains of the skate and human and a new putative antigen binding molec
8                           How have North Sea skate and shark assemblages changed since the early 20th
9                             Pectoral fins of skates and rays, such as the little skate (Batoid, Leuco
10 hal versus 1.1 to 20 for ringed seal, arctic skate, and beluga whale, respectively).
11                  Cartilaginous fish (sharks, skates, and rays) are in the oldest taxon of extant jawe
12 r organization in elasmobranch fish (sharks, skates, and rays) differs from that in other vertebrates
13 lved at all swimming speeds in the clearnose skate; and (iii) critical swimming protocols might misre
14                                   Sharks and skates are representatives of the earliest vertebrates w
15 ewer recreational activities such as in-line skating, are rapidly gaining the recognition they deserv
16  fins of skates and rays, such as the little skate (Batoid, Leucoraja erinacea), show a strikingly un
17 nic anions and steroids, including the major skate bile salt, scymnol sulfate.
18                          In addition, in the skate but not the rat retina, retinal pigment epithelial
19 gous sequences from tetrapods, zebrafish and skate can drive reporter gene expression in mouse limbs
20 nel and rectifying Kv channel predicted from skate (cartilaginous fish) ampullary organ electrophysio
21  long-term declines, and the largest (common skate complex) became locally extirpated (as did angelsh
22  family revealed that perch Cx35 and Cx34.7, skate Cx35, and mouse Cx36 constitute a novel gamma subg
23 critically endangered species such as common skate (Dipturus batis) and angelshark (Squatina squatina
24             Upon hypotonic volume expansion, skate erythrocytes lose solutes via a pathway that requi
25                                              Skate erythrocytes possess numerous tyrosine kinases inc
26                Hypotonic volume expansion of skate erythrocytes rapidly stimulates the tyrosine phosp
27 OSTalpha-OSTbeta pairs from human, mouse, or skate) generated robust estrone 3-sulfate transport acti
28                                              Skate hepatocyte cDNA was amplified with degenerate olig
29  protein in the KI-IOV was identified as the skate homolog of the mammalian red cell anion exchanger
30 an unusual Sec tail, which is orthologous to skate IgX(short) cDNA.
31 22.5 million people participating in in-line skating in the United States in 1995, about 100,000 were
32 rentiation; it is found, in both the rat and skate, in the ventricular space that ultimately becomes
33 w pads, knee pads, and helmets in preventing skating injuries.
34 clasper development from pelvic fins of male skates is controlled by hormonal regulation of the Sonic
35     Further analyses showed that microtubule skating is a form of one-dimensional diffusion along the
36 s of the shark Scyliorhinus canicula and the skate Leucoraja erinacea and the absence of all HoxC gen
37 nts of the jaw, hyoid and gill arches of the skate Leucoraja erinacea derive from molecularly equival
38  expressed by electrosensory cells in little skate (Leucoraja erinacea) and functionally couple to me
39 he gills of a cartilaginous fish, the little skate (Leucoraja erinacea), are in fact endodermally der
40  embryos of a cartilaginous fish, the little skate (Leucoraja erinacea).
41  DiI tracing for up to 70 days in the little skate, Leucoraja erinacea, we show that lateral line pla
42 ction product was found and used to screen a skate liver cDNA library.
43                                    Thus, the skate liver P2Y receptor functions as a primitive P2Y AT
44 y analysis of nucleotide alignments show the skate opsin to be homologous to other rod opsins.
45 the similarity of the cytoplasmic domains of skate opsin to those of blue-sensitive visual pigments.
46 n action resembling that of flatfish such as skates or rays.
47                                              Skate orthologs of mammalian GATA-3, GATA-1, EBF-1, Pax-
48                          Srds represents the skate orthologue of mammalian peripherin/rds genes.
49                            Human, mouse, and skate OSTalpha proteins are predicted to contain seven t
50  human P2Y(2), rat P2Y(6), human P2Y(11), or skate P2Y receptors in oocytes resulted in modulation of
51 ply ancestral patterns of gene expression in skate pectoral fins, shedding light on the molecular mec
52    The 5' and 3' untranslated regions of the skate peripherin/rds (srds) cDNA were isolated by the ra
53    To determine the cellular function of the skating phenomenon, dynein and the dynactin microtubule-
54       Cartilaginous fishes (e.g., sharks and skates) possess a postcranial dermal skeleton consisting
55 to functionally complement the corresponding skate proteins by measuring transport of [3H]estrone 3-s
56                        The all-rod retina of skate provides a comparatively simple system in which to
57   The tissue-specific expression patterns of skate PU.1 and Spi-C suggest that these genes share regu
58 s are highly conserved between mammalian and skate PU.1, in marked contrast to lamprey Spi, in which
59 sed a negatively buoyant fish, the clearnose skate Raja eglanteria, and took two approaches: a classi
60 heteroclitus), two elasmobranch species (the skate Raja erinacea and the dogfish Mustelus canis), and
61 ce suggests that hepatocytes from the little skate Raja erinacea express a primitive P2Y ATP receptor
62 rily primitive marine vertebrate, the little skate Raja erinacea, was screened for taurocholate trans
63 t diverging jawed vertebrates, the clearnose skate (Raja eglanteria).
64                   Volume expansion of little skate (Raja erinacea) erythrocytes increases the affinit
65                                              Skates (Raja erinacea and R. ocellata) are among the few
66 a proteins recently identified in the little skate, Raja erinacea, even though the latter exhibit onl
67                                In the little skate, Raja erinacea, the electrosensory primary afferen
68                     Chondrichthyans (sharks, skates, rays and holocephalans) possess paired appendage
69 ep in the volume-activated taurine efflux in skate red cells.
70                                   Sharks and skates represent the earliest vertebrates with an adapti
71 ast two of the four Ikaros family members in skate resemble the patterns observed in mammals, i.e., i
72       Both immunohistochemistry in the adult skate retina and in situ hybridizations in the adult rat
73 ve cloned and analyzed the opsin cDNA from a skate retina library.
74  molecular basis of visual adaptation in the skate retina, we have cloned and analyzed the opsin cDNA
75 uxes from horizontal cells isolated from the skate retina.
76                                            A skate retinal cDNA library was screened using a mouse pe
77 ue of peripherin/rds was identified from the skate retinal cDNA library.
78 bridization to clone a novel connexin from a skate retinal cDNA library.
79  indicate alterations in the interactions of skate rhodopsin with other proteins in the phototransduc
80                                     However, skate rods are unusual in that they are capable of adapt
81 in the posterior half of the pectoral fin of skate, shark, and zebrafish but in the anterior side of
82 enerate primers and R. eglanteria (clearnose skate) spleen cDNA as template.
83         The receptor was expressed widely in skate tissue and was expressed to a similar extent in ot
84 on and fate-mapping approaches in the little skate to demonstrate that Shh secretion from a signallin
85 mobranch fishes, including sharks, rays, and skates, use specialized electrosensory organs called amp
86  had and whether or not they performed trick skating, was 9.5 (95 percent confidence interval, 2.6 to
87 rovided by batoid fish such as stingrays and skates, we created a biohybrid system that enables an ar
88 earned a motor skill, such as cycling or ice-skating, we can rapidly generalize to novel tasks, such
89 ically isolated external horizontal cells of skate were examined using whole-cell voltage-clamp techn

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